Salman F Bhai

10PUBLICATIONS
27CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Metabolic medicinePacific Peoples and disabilityNeurology and neuromuscular diseasesDevelopmental genetics (incl. sex determination)
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Publications (10)

|Sep 27, 2025
Rhabdomyolysis in the Era of Next-Generation Sequencing: Selecting Patients with a High Likelihood of a Genetic Susceptibility Using 'RHABDO' Features.

Nick Kruijt, Sanne A J H van de Camp, Jasper J Kramer

|Apr 03, 2025
Diagnosis of Primary Mitochondrial Diseases.

Salman Bhai, Michio Hirano

|Mar 26, 2025
The caregiver burden of idiopathic inflammatory myopathies.

Parker Brady, Roberto Sergio Hernandez, Amber Salter

|Nov 11, 2024
Experiences of living with GSD5 (McArdle) disease: challenges and strategies. A qualitative study in the Netherlands.

Ronne van Haaren-Pater, Walaa Karazi, Daphne Maas

|Nov 08, 2024
A 40-week phase 2B randomized, multicenter, double-blind, placebo-controlled study evaluating the safety and efficacy of memantine in amyotrophic lateral sclerosis.

Salman Bhai, Todd Levine, Dan Moore

|Jul 23, 2024
Diagnostic workup of rhabdomyolysis: Genetic testing should precede neurophysiological testing.

Nicol C Voermans, Salman Bhai, Pascal Laforet

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Frequent Collaborators

2 joint publications

Nicol C Voermans

1 joint publications

Andrew J Heim

1 joint publications

Zachary Simmons

1 joint publications

Tiffany Schwasinger-Schmidt